IP Library Patent Application 18802256
Patent Application
App. No. 18/802,256

MOLECULES HAVING PESTICIDAL UTILITY, AND INTERMEDIATES, COMPOSITIONS, AND PROCESSES, RELATED THERETO

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Quick Facts
Patent No.
US None
App. No.
18/802,256
Abstract

This disclosure relates to the field of molecules having pesticidal utility against pests in Phyla Arthropoda, Mollusca, and Nematoda, processes to produce such molecules, intermediates used in such processes, pesticidal compositions containing such molecules, and processes of using such pesticidal compositions against such pests. These pesticidal compositions may be used, for example, as acaricides, insecticides, miticides, molluscicides, and nematicides. This document discloses molecules having the following formula (“Formula One”).

Claims (87)

1 .- 4 . (canceled)

5 . A molecule selected from one of the molecules listed in the following Table.

No.

Structure

F24

F63

F64

F65

F75

F180

F187

F203

F211

F241

F242

F247

F252

F281

F297

F306

F309

F310

F311

F312

F316

F319

F330

F331

F342

F351

F352

F353

F354

F357

F383

F385

F386

F389

F390

F391

F392

F395

F396

F397

F398

F399

F400

F414

F533

F541

F542

F543

F546

F547

F548

F549

F552

F553

F558

F559

F560

F561

F562

F563

F564

F565

F566

F572

F580

F584

F585

F586

F587

F588

F589

F590

F591

PF6

PF39

6 . A molecule according to claim 5 , wherein the carboxamido, and the phenyl, which are bonded to the cyclopropane, are in the R,R configuration.

7 . A composition comprising a molecule according to any of the previous claims further comprises a carrier and/or an active ingredient.

8 . A composition according to claim 7 , the composition further comprises an active ingredient selected from acaricides, algicides, antifeedants, avicides, bactericides, bird repellents, chemosterilants, fungicides, herbicide safeners, herbicides, insect attractants, insect repellents, insecticides, mammal repellents, mating disrupters, molluscicides, nematicides, plant activators, plant growth regulators, rodenticides, synergists, and virucides, an active ingredient selected from AIGA, AI-1, AI-2, or AIGA-2, or further comprising Lotilaner, a molecule selected from Table A, or a biopesticide.

9 . A composition according to claim 7 , the composition further comprises an active ingredient from Acetylcholinesterase (AChE) inhibitors; GABA-gated chloride channel antagonists; Sodium channel modulators; Nicotinic acetylcholine receptor (nAChR) agonists; Nicotinic acetylcholine receptor (nAChR) allosteric activators; Chloride channel activators; Juvenile hormone mimics; Miscellaneous nonspecific (multi-site) inhibitors; Modulators of Chordotonal Organs; Mite growth inhibitors; Microbial disruptors of insect midgut membranes; Inhibitors of mitochondrial ATP synthase; Uncouplers of oxidative phosphorylation via disruption of the proton gradient; Nicotinic acetylcholine receptor (nAChR) channel blockers; Inhibitors of chitin biosynthesis, type 0; Inhibitors of chitin biosynthesis, type 1; Moulting disruptor, Dipteran; Ecdysone receptor agonists; Octopamine receptor agonists; Mitochondrial complex III electron transport inhibitors; Mitochondrial complex I electron transport inhibitors; Voltage-dependent sodium channel blockers; Inhibitors of acetyl CoA carboxylase; Mitochondrial complex IV electron transport inhibitors; Mitochondrial complex II electron transport inhibitors; Ryanodine receptor modulators; or Group UN.

10 . A composition according to any one of claims 7-9 , wherein the weight ratio of the molecule selected from the Table to the active ingredient is 100:1 to 1:100, 50:1 to 1:50, 20:1 to 1:20, 10:1 to 1:10, 5:1 to 1:5, 3:1 to 1:3, 2:1 to 1:2, or 1:1; and/or wherein the weight ratio of the molecule selected from the Table to the active ingredient is X:Y; wherein X is the parts by weight of the molecule selected from the Table and Y is the parts by weight of the active ingredient; further wherein the numerical range of the parts by weight for X is 0<X≤100 and the parts by weight for Y is 0<Y≤100; and further wherein X and Y are selected from Table C, optionally wherein a range of weight ratios of the molecule selected from the Table to the active ingredient is X 1 :Y 1 , to X 2 :Y 2 ; further wherein X 1 >Y 1 and X 2 <Y 2 ; or wherein X 1 >Y 1 and X 2 >Y 2 ; or wherein X 1 <Y 1 and X 2 <Y 2 .

11 . A process to control a pest, wherein the process comprises applying to a locus, a pesticidally effective amount of a molecule according to any one of claims 5-7 or a composition according to any one of claims 7-10 .

12 . A process according to claim 11 wherein the pest is selected from the group consisting of ants, aphids, bed bugs, beetles, bristletails, caterpillars, cockroaches, crickets, carwigs, fleas, flies, grasshoppers, grubs, leafhoppers, lice, locusts, maggots, mites, nematodes, planthoppers, psyllids, sawflies, scales, silverfish, slugs, snails, spiders, springtails, stink bugs, symphylans, termites, thrips , ticks, wasps, whiteflies, and wireworms.

13 . A process according claim 11 wherein the pest is a sap-feeding pest or a chewing pest; or wherein the pest is selected from the group consisting of aphids, leafhoppers, moths, scales, thrips , psyllids, mealybugs, stinkbugs, and whiteflies; or from the group consisting of caterpillars, beetles, grasshoppers, and locusts; or wherein the pest is selected from the group consisting of Orders Anoplura and Hemiptera; or from the group consisting of Coleoptera and Lepidoptera; or wherein the pest is selected from the group consisting of Aulacaspis spp., Aphrophora spp., Aphis spp., Bemisia spp., Coccus spp., Euschistus spp., Lygus spp., Macrosiphum spp., Nezara spp., and Rhopalosiphum spp; or from the group consisting of Anthonomus spp., Cerotoma spp., Chaetocnema spp., Colaspis spp., Cyclocephala spp., Diabrotica spp., Hypera spp., Phyllophaga spp., Phyllotreta spp., Sphenophorus spp., and Sitophilus spp.